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Brunner-Krainz, M.
~ 0
results:
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Format
Online
Mediatypes
Articles (Online)
Bookchapter (Online)
OpenAccess-fulltext
Languages
english (35)
german (4)
Sorted by: Relevance
Sorted by: Year
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1
Epileptic phenotypes, electroclinical features and clinical..:
Haberlandt, E.
;
Ensslen, M.
;
Gruber-Sedlmayr, U.
...
European Journal of Paediatric Neurology. 21 (2017) 3 - p. 457-464 , 2017
Link:
https://doi.org/10.1016/..
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2
Pompe disease in Austria: clinical, genetic and epidemiolog..:
Löscher, W. N.
;
Huemer, M.
;
Stulnig, T. M.
...
Journal of Neurology. 265 (2017) 1 - p. 159-164 , 2017
Link:
https://doi.org/10.1007/..
?
3
Leitlinien zur Ernährung in der pädiatrischen Palliativmedi..:
Jones, R.
;
Behrens, R.
;
Brunner-Krainz, M.
...
Pädiatrie & Pädologie. 50 (2015) S1 - p. 4-24 , 2015
Link:
https://doi.org/10.1007/..
?
4
Konsensus zur Ernährung in der pädiatrischen Palliativmediz..:
Jones, R.
;
Behrens, R.
;
Dilch, A.
...
Monatsschrift Kinderheilkunde. 163 (2015) 9 - p. 928-933 , 2015
Link:
https://doi.org/10.1007/..
?
5
Persisting myelin oligodendrocyte glycoprotein antibodies i..:
Rostásy, K
;
Mader, S
;
Hennes, EM
...
Multiple Sclerosis Journal. 19 (2012) 8 - p. 1052-1059 , 2012
Link:
https://doi.org/10.1177/..
?
6
Efficacy and safety of empagliflozin in glycogen storage di..:
Grünert, S.C
;
Derks, TGJ
;
Adrian, K
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.gim.2022.04.001. , 2022
Link:
https://serval.unil.ch/n..
?
7
A generic emergency protocol for patients with inborn error..:
Rossi, A
;
Hoogeveen, IJ
;
Lubout, CMA
...
https://discovery.ucl.ac.uk/id/eprint/10149887/1/J%20of%20Inher%20Metab%20Disea%20-%202021%20-%20Rossi%20-%20A%20generic%20emergency%20protocol%20for%20patients%20with%20inborn%20errors%20of%20metabolism%20causing.pdf. , 2021
Link:
https://discovery.ucl.ac..
?
8
Epileptic phenotypes, electroclinical features and clinical..:
Haberlandt, E
;
Ensslen, M
;
Gruber-Sedlmayr, U
...
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/111693. , 2017
Link:
https://opus.bibliothek...
?
9
Combined respiratory chain deficiency and UQCC2 mutations i..:
Feichtinger, R.G
;
Brunner-Krainz, M
;
Alhaddad, B
...
info:eu-repo/semantics/altIdentifier/doi/10.1155/2017/7202589. , 2017
Link:
https://push-zb.helmholt..
?
10
Propionic acidemia: clinical course and outcome in 55 pedia..:
Grünert, S.C
;
Müllerleile, S
;
De Silva, L
...
info:eu-repo/semantics/altIdentifier/doi/10.1186/1750-1172-8-6. , 2013
Link:
https://serval.unil.ch/n..
?
11
Epilepsie als Leitsymptom angeborener Stoffwechselstörungen:
Plecko B
;
Brunner-Krainz M
;
Gruber-Sedlmayr U
.
http://www.kup.at/kup/pdf/5525.pdf. , 2005
Link:
http://www.kup.at/kup/pd..
?
12
Ketogenic Diet Treatment of Defects in the Mitochondrial Ma..:
Bölsterli, Bigna K.
;
Boltshauser, Eugen
;
Palmieri, Luigi
...
Nutrients. 14 (2022) 17 - p. 3605 , 2022
Link:
https://doi.org/10.3390/..
?
13
Combined Respiratory Chain Deficiency and UQCC2 Mutations i..:
Feichtinger, René G.
;
Brunner-Krainz, Michaela
;
Alhaddad, Bader
...
Oxidative Medicine and Cellular Longevity. 2017 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1155/..
?
14
Clinical outcome, biochemical and therapeutic follow-up in ..:
Karall, Daniela
;
Brunner-Krainz, Michaela
;
Kogelnig, Katharina
...
Orphanet Journal of Rare Diseases. 10 (2015) 1 - p. , 2015
Link:
https://doi.org/10.1186/..
?
15
Ketogenic Diet Treatment of Defects in the Mitochondrial Ma..:
Bölsterli, Bigna, K
;
Boltshauser, Eugen
;
Palmieri, Luigi
...
info:eu-repo/semantics/altIdentifier/doi/10.3390/nu14173605. , 2022
Link:
https://hal.science/hal-..
1-15